次要组织相容性抗原差异对hla匹配的同胞供体造血干细胞移植结果的发生及影响

Bone Marrow Research Pub Date : 2012-01-01 Epub Date: 2012-11-08 DOI:10.1155/2012/257086
Monika Dzierzak-Mietla, M Markiewicz, Urszula Siekiera, Sylwia Mizia, Anna Koclega, Patrycja Zielinska, Malgorzata Sobczyk-Kruszelnicka, Slawomira Kyrcz-Krzemien
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引用次数: 22

摘要

我们检测了11种次要组织相容性抗原(MiHA)的等位基因,并调查了2000年至2008年间62例同种异体造血细胞移植(allogeneic hematopoietic cell transplantation,同种异体造血细胞移植)的骨髓清除条件和其hla匹配的兄弟供体中免疫原性MiHA差异的发生。在42对供受体中检测到免疫原性MiHA错配:29%的MiHA在HVG方向错配,29%的MiHA在GVH方向错配;10%检测到双向MiHA差异,32%检测到无MiHA不匹配。gvh导向HY错配患者的3年总生存期和无病生存期均低于兼容HY患者;此外,在gvh导向的HY不匹配的患者中,观察到严重急性GvHD和广泛慢性GvHD的发生率更高。相反,gvh导向的常编码MiHAs错配对总体生存没有负面影响。我们的研究结果有助于理解为什么尽管供体和受体的HLA完全匹配,但来自兄弟姐妹的同种异体hct的移植后病程可能会有所不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Occurrence and Impact of Minor Histocompatibility Antigens' Disparities on Outcomes of Hematopoietic Stem Cell Transplantation from HLA-Matched Sibling Donors.

Occurrence and Impact of Minor Histocompatibility Antigens' Disparities on Outcomes of Hematopoietic Stem Cell Transplantation from HLA-Matched Sibling Donors.

Occurrence and Impact of Minor Histocompatibility Antigens' Disparities on Outcomes of Hematopoietic Stem Cell Transplantation from HLA-Matched Sibling Donors.

Occurrence and Impact of Minor Histocompatibility Antigens' Disparities on Outcomes of Hematopoietic Stem Cell Transplantation from HLA-Matched Sibling Donors.

We have examined the alleles of eleven minor histocompatibility antigens (MiHAs) and investigated the occurrence of immunogenic MiHA disparities in 62 recipients of allogeneic hematopoietic cell transplantation (allo-HCT) with myeloablative conditioning performed between 2000 and 2008 and in their HLA-matched sibling donors. Immunogenic MiHA mismatches were detected in 42 donor-recipient pairs: in 29% MiHA was mismatched in HVG direction, in another 29% in GVH direction; bidirectional MiHA disparity was detected in 10% and no MiHA mismatches in 32%. Patients with GVH-directed HY mismatches had lower both overall survival and disease-free survival at 3 years than patients with compatible HY; also higher incidence of both severe acute GvHD and extensive chronic GVHD was observed in patients with GVH-directed HY mismatch. On contrary, GVH-directed mismatches of autosomally encoded MiHAs had no negative effect on overall survival. Results of our study help to understand why posttransplant courses of allo-HCT from siblings may vary despite the complete high-resolution HLA matching of a donor and a recipient.

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